Bowne, S. J., Sullivan, L. S., Blanton, S. H., Cepko, C. L., Blackshaw, S., Birch, D. G., . . . Daiger, S. P. (2002). Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.
Citação norma ChicagoBowne, Sara J., Lori S. Sullivan, Susan H. Blanton, Constance L. Cepko, Seth Blackshaw, David G. Birch, Dianna Hughbanks-Wheaton, John R. Heckenlively, and Stephen P. Daiger. Mutations in the Inosine Monophosphate Dehydrogenase 1 Gene (IMPDH1) Cause the RP10 Form of Autosomal Dominant Retinitis Pigmentosa. 2002.
MLA citiranjeBowne, Sara J., et al. Mutations in the Inosine Monophosphate Dehydrogenase 1 Gene (IMPDH1) Cause the RP10 Form of Autosomal Dominant Retinitis Pigmentosa. 2002.